Canonical Allele Identifier: CA389225948

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709870C>G (hg19) ; chr14:g.24240664C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240664C>G , CM000676.2:g.24240664C>G	GRCh38
NC_000014.8:g.24709870C>G , CM000676.1:g.24709870C>G	GRCh37
NC_000014.7:g.23779710C>G	NCBI36
NG_016650.1:g.7011G>C
NG_054634.1:g.13248C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1119G>C
ENST00000557921.3:c.708G>C	ENSP00000453157.3:p.Trp236Cys
ENST00000699682.1:n.1206G>C
ENST00000699683.1:n.1256G>C
ENST00000699684.1:c.*409G>C	ENSP00000514523.1:n.*409G>C
ENST00000699685.1:n.1020G>C
ENST00000699686.1:c.609G>C	ENSP00000514524.1:p.Trp203Cys
ENST00000699687.1:c.711G>C	ENSP00000514525.1:p.Trp237Cys
ENST00000699688.1:n.1016G>C
ENST00000699689.1:n.1372G>C
ENST00000699690.1:n.1569G>C
ENST00000699691.1:n.1713G>C
ENST00000699693.1:n.1233G>C
ENST00000699694.1:n.1475G>C
ENST00000699695.1:c.*188G>C	ENSP00000514526.1:n.*188G>C
ENST00000699696.1:n.1119G>C
ENST00000699697.1:c.816G>C	ENSP00000514527.1:p.Trp272Cys
ENST00000699698.1:n.737G>C
ENST00000699699.1:n.1140G>C
ENST00000699700.1:n.1263G>C
ENST00000699701.1:c.*196G>C	ENSP00000514528.1:n.*196G>C
ENST00000267415.12:c.816G>C MANE Select	ENSP00000267415.7:p.Trp272Cys
ENST00000557921.2:c.708G>C	ENSP00000453157.2:p.Trp236Cys
ENST00000646753.1:c.711G>C	ENSP00000494065.1:p.Trp237Cys
ENST00000267415.11:c.816G>C	ENSP00000267415.7:p.Trp272Cys
ENST00000399423.8:c.816G>C	ENSP00000382350.4:p.Trp272Cys
ENST00000558476.5:c.378G>C	ENSP00000452724.1:p.Trp126Cys
ENST00000558566.1:c.*188G>C	ENSP00000453025.1:n.*188G>C
ENST00000559019.1:c.*188G>C	ENSP00000453675.1:n.*188G>C
ENST00000559549.1:n.542G>C
ENST00000559969.5:c.757+15G>C
ENST00000626689.2:c.*188G>C	ENSP00000486681.1:n.*188G>C
NM_001099274.1:c.816G>C	NP_001092744.1:p.Trp272Cys
NM_012461.2:c.816G>C	NP_036593.2:p.Trp272Cys
XM_005267528.2:c.816G>C	XP_005267585.1:p.Trp272Cys
XM_005267529.2:c.711G>C	XP_005267586.1:p.Trp237Cys
NM_001099274.2:c.816G>C	NP_001092744.1:p.Trp272Cys
NM_001363668.1:c.711G>C	NP_001350597.1:p.Trp237Cys
NM_012461.3:c.816G>C	NP_036593.2:p.Trp272Cys
XM_011536642.2:c.*196G>C	XP_011534944.1:n.*196G>C
XM_017021216.2:c.174G>C	XP_016876705.1:p.Trp58Cys
XM_017021217.1:c.174G>C	XP_016876706.1:p.Trp58Cys
NM_001099274.3:c.816G>C MANE Select	NP_001092744.1:p.Trp272Cys
NM_001363668.2:c.711G>C	NP_001350597.1:p.Trp237Cys